A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2855401



Internal ID15697647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:196856007..196926935hg38UCSC Ensembl
Innerchr1:196825137..196896065hg19UCSC Ensembl
Innerchr1:195091760..195162688hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3870929
hg1970929
hg1870929
Variant TypeCNV loss
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514032
Supporting Variants
SamplesNA18870
Known GenesCFHR4
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2855401
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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